7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine

Base Information

• Chemical Name: 7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine
• CAS No.: 885280-71-7
• Molecular Formula: C₁₀H₁₂BrN
• Molecular Weight: 226.116
• Hs Code.: 2921450090
• DSSTox Substance ID: DTXSID30595737
• Mol file: 885280-71-7.mol

Synonyms:7-bromo-1,2,3,4-tetrahydronaphthalen-2-amine;885280-71-7;7-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YLAMINE;7-bromotetralin-2-amine;SCHEMBL415207;SCHEMBL445089;7-BROMO-1,2,3,4-TETRAHYDRO-2-NAPHTHALENAMINE;DTXSID30595737;PNTPMWBRGXAFII-UHFFFAOYSA-N;MFCD06739164;AKOS024260310;AB10494;AB28750;CS-W006544;AS-44497;DB-077850;A842671;J-519095;7-Bromo-1 pound not2 pound not3 pound not4-tetrahydronaphthalen-2-amine

Chemical Property of 7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine

Chemical Property:

• Boiling Point: 298.7±40.0 °C(Predicted)
• PKA: 10.03±0.20(Predicted)
• PSA: 26.02000
• Density: 1.413±0.06 g/cm3(Predicted)
• LogP: 2.96540
• Storage Temp.: 2-8°C(protect from light)
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 225.01531
• Heavy Atom Count: 12
• Complexity: 160

Purity/Quality:

97% ^*data from raw suppliers

7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2=C(CC1N)C=C(C=C2)Br

Technology Process of 7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine

There total 1 articles about 7-Bromo-1,2,3,4-tetrahydronaphthalen-2-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

7-bromo-2-tetralone (132095-54-6) → 7-bromo-1,2,3,4-tetrahydro-naphthalen-2-ylamine (885280-71-7)

Guidance literature:

With ammonium acetate; sodium cyanoborohydride; In methanol; at 20 ℃;

Reference yield:

7-bromo-1,2,3,4-tetrahydro-naphthalen-2-ylamine (885280-71-7) → 3-(4-fluoroanilino)tetralin-6-carbohydroxamic acid (1364164-16-8)

Guidance literature:

Multi-step reaction with 5 steps

1: triethylamine / ethanol / 2 h / 20 °C

2: 1,3-bis-(diphenylphosphino)propane; palladium diacetate / N,N-dimethyl-formamide / 12 h / 80 °C

3: hydrogenchloride / water; methanol / 1 h / 20 °C

4: triethylamine / L-proline; copper(l) iodide / N,N-dimethyl-formamide / 0.5 h / 120 °C / microwave irradiation

5: potassium hydroxide; hydroxylamine / water; methanol / 1 h / 20 °C

With hydrogenchloride; hydroxylamine; triethylamine; potassium hydroxide; copper(l) iodide; 1,3-bis-(diphenylphosphino)propane; palladium diacetate; L-proline; In methanol; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

7-bromo-1,2,3,4-tetrahydro-naphthalen-2-ylamine (885280-71-7) → C18H18FNO2 (1364165-64-9)

Guidance literature:

Multi-step reaction with 4 steps

1: triethylamine / ethanol / 2 h / 20 °C

2: 1,3-bis-(diphenylphosphino)propane; palladium diacetate / N,N-dimethyl-formamide / 12 h / 80 °C

3: hydrogenchloride / water; methanol / 1 h / 20 °C

4: triethylamine / L-proline; copper(l) iodide / N,N-dimethyl-formamide / 0.5 h / 120 °C / microwave irradiation

With hydrogenchloride; triethylamine; copper(l) iodide; 1,3-bis-(diphenylphosphino)propane; palladium diacetate; L-proline; In methanol; ethanol; water; N,N-dimethyl-formamide;

upstream raw materials:

7-bromo-2-tetralone

Downstream raw materials:

3-(4-fluoroanilino)tetralin-6-carbohydroxamic acid

C₁₈H₁₈FNO₂

3-[(3-fluorophenyl)sulfonylamino]tetralin-6-carbohydroxamic acid

7-(4-Chloro-benzenesulfonylamino)-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid hydroxyamide

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